N. Koga et al., ANALYSIS OF THE BIOH GENE OF ESCHERICHIA-COLI AND ITS EFFECT ON BIOTIN PRODUCTIVITY, Journal of fermentation and bioengineering, 81(6), 1996, pp. 482-487
The bioH gene, which is obligatory for biotin biosynthesis in Escheric
hia coli, was isolated as an 11-kb EcoRI fragment from E. coli by comp
lementation for the growth of the bioH mutant. Deletion analysis of th
is fragment showed that the bioH gene was located within the 3.3-kb Ec
oRI-EcoRV fragment. Sequencing this fragment revealed the presence of
two open reading frames, and a further complementation test showed tha
t one of them codes for this gene. The molecular weight of the bioH ge
ne product was about 25-kDa by the maxicell method, which was in good
accordance with the molecular weight from the predicted nucleotide seq
uence. The promoter region of the bioH gene had no significant homolog
y with that of the biotin operon and no operator sequence for the bind
ing of the repressor protein (birA). LacZ-fusion analysis showed that
the activity of this bioH promoter was not repressed by biotin, sugges
ting that the gene expression of the bioH is not regulated by the birA
gene product, which acts as a repressor of the biotin operon. We atte
mpted to increase the biotin productivity by the introducing the bioH
gene into a high-copy plasmid in the presence of the biotin operon, bu
t the productivity of the biotin and biotin intermediates (total bioti
n) significantly decreased. This indicated that the overexpression of
the bioH gene reduces the level of a biotin precursor, although it is
required for biotin biosynthesis.